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3. Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation. Harding AE; Sweeney MG; Miller DH; Mumford CJ; Kellar-Wood H; Menard D; McDonald WI; Compston DA Brain; 1992 Aug; 115 ( Pt 4)():979-89. PubMed ID: 1393514 [TBL] [Abstract][Full Text] [Related]
5. Mitochondrial mutations of Leber's hereditary optic neuropathy: a risk factor for multiple sclerosis. Vanopdenbosch L; Dubois B; D'Hooghe MB; Meire F; Carton H J Neurol; 2000 Jul; 247(7):535-43. PubMed ID: 10993496 [TBL] [Abstract][Full Text] [Related]
6. Leber's hereditary optic neuropathy mitochondrial DNA mutations at nucleotides 11778 and 3460 in multiple sclerosis. Mojon DS; Herbert J; Sadiq SA; Miller JR; Madonna M; Hirano M Ophthalmologica; 1999; 213(3):171-5. PubMed ID: 10202290 [TBL] [Abstract][Full Text] [Related]
7. Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis. Kellar-Wood H; Robertson N; Govan GG; Compston DA; Harding AE Ann Neurol; 1994 Jul; 36(1):109-12. PubMed ID: 8024249 [TBL] [Abstract][Full Text] [Related]
16. De novo 14484 mitochondrial DNA mutation in monozygotic twins discordant for Leber's hereditary optic neuropathy. Biousse V; Brown MD; Newman NJ; Allen JC; Rosenfeld J; Meola G; Wallace DC Neurology; 1997 Oct; 49(4):1136-8. PubMed ID: 9339703 [TBL] [Abstract][Full Text] [Related]
17. The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy. Chinnery PF; Brown DT; Andrews RM; Singh-Kler R; Riordan-Eva P; Lindley J; Applegarth DA; Turnbull DM; Howell N Brain; 2001 Jan; 124(Pt 1):209-18. PubMed ID: 11133798 [TBL] [Abstract][Full Text] [Related]
18. Hereditary cerebellar ataxia with Leber's hereditary optic neuropathy mitochondrial DNA 11778 mutation. Murakami T; Mita S; Tokunaga M; Maeda H; Ueyama H; Kumamoto T; Uchino M; Ando M J Neurol Sci; 1996 Oct; 142(1-2):111-3. PubMed ID: 8902729 [TBL] [Abstract][Full Text] [Related]
19. A multiple sclerosis-like illness in a man harboring the mtDNA 14484 mutation. Bhatti MT; Newman NJ J Neuroophthalmol; 1999 Mar; 19(1):28-33. PubMed ID: 10098545 [TBL] [Abstract][Full Text] [Related]
20. No genetic differences between affected and unaffected members of a German family with Leber's hereditary optic neuropathy (LHON) with respect to ten mtDNA point mutations associated with LHON. Gerbitz KD; Paprotta A; Obermaier-Kusser B; Rietschel M; Zerres K FEBS Lett; 1992 Dec; 314(3):251-5. PubMed ID: 1361456 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]